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MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM

K873332 Class I Traditional
Decision Date
1987-09-08
Sponsor / Applicant
American V. Mueller

Technical Specification

510(k) Submission ID K873332
Product Code GCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4680
Decision Date 1987-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM received FDA 510(k) clearance under submission number K873332, sponsored by American V. Mueller. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1987-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code GCY and 21 CFR 878.4680, within the General, Plastic Surgery review panel as a Class I device.